1)      Bezzina, Connie., et al. “Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in Conduction Systems.” Circulation Research 2003 Feb 7; 92(2):159-68.


2)      Cardio Update. “Long QT syndrome.” 2002. Sibley Heart Center Cardiology.


3)      Clancy. Colleen E., et al. “Insights into the molecular mechanisms of bradcardia-triggered arrhythmias in long QT3 syndrome.” The Journal of Clinical Investigation. 2002 Nov. Vol 110.


4)      “Long QT Syndrome (LQT).” Cleveland Clinic Heart Center. 3 May 2003.


5)      Marx, Jean. “Gene Mutation May Boost Risk of Heart Arrhythmias.” Science Magazine. Vol 297. (2002): 23 Aug. 2002.


6)      Neuromuscular Disease Center. ION CHANNELS, TRANSMITTERS, RECEPTORS & DISEASE. 10 Feb 2000.


7) 2002.


8)      Online Mendelian Inheritance in Man. LONG QT SYNDROME 3; LQT3. 5 Feb 2003. NCBI.


9)      Ravina, Thomas. Lapuerta, Jose A. and Brugada, Josep.  “Prolonged repolarization in long QT3 syndrome: unusual electrocardiographic findings.” International Journal of Cardiology 82 (2002): 71-73.


10)  Splawski, Igor., et al. “Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia.” Science Magazine. Vol 297 23 Aug. 2002